NDC 71335-9692 – Pravastatin Sodium

Pravastatin Sodium 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-9692

Product details

Brand name
Pravastatin Sodium
Generic name
Pravastatin Sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209869
Marketed since
February 1, 2021
Listing expires
December 31, 2027
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pravastatin Sodium →

Package NDC codes (5)

Package NDCDescriptionSince
71335-9692-130 TABLET in 1 BOTTLE (71335-9692-1)Apr 18, 2023
71335-9692-290 TABLET in 1 BOTTLE (71335-9692-2)Apr 18, 2023
71335-9692-3100 TABLET in 1 BOTTLE (71335-9692-3)Apr 18, 2023
71335-9692-460 TABLET in 1 BOTTLE (71335-9692-4)Apr 18, 2023
71335-9692-510 TABLET in 1 BOTTLE (71335-9692-5)Apr 18, 2023

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